Canonical Allele Identifier: CA1522520679
Gene: SLC6A19 HGNC NCBI

Linked Data

dbSNP Id: rs1746124279
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213847C>T , CM000667.2:g.1213847C>T GRCh38
NC_000005.9:g.1213962C>T , CM000667.1:g.1213962C>T GRCh37
NC_000005.8:g.1266962C>T NCBI36
NG_008282.1:g.17253C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.775-106C>T MANE Select ENSP00000305302.10:n.775-106C>T
ENST00000304460.10:c.775-106C>T ENSP00000305302.10:n.775-106C>T
ENST00000515652.5:c.683-106C>T ENSP00000425701.1:n.683-106C>T
NM_001003841.2:c.775-106C>T NP_001003841.1:n.775-106C>T
NM_001003841.3:c.775-106C>T MANE Select NP_001003841.1:n.775-106C>T
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